Canonical Allele Identifier: PA120779
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 9847
ClinVar RCV Id: RCV000010521 RCV003133116
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000035.2:p.Met808Thr
CA120777
NM_000044.6:c.2423T>C